Brais B - Search Results

1

White matter abnormalities in 15 subjects with SPG76.

Alkhalifa A, Chen S, Hasiloglu ZI, Filosto M, Cali E, Houlden H, Sgobbi de Souza P, Alavi A, Goizet C, Stevanin G, Taithe F, Nicita F, Vasco G, Tozza S, Cocozza S, Carboni N, Figus A, Wu J, Basak AN, Brais B, Rouleau G, La Piana R. Alkhalifa A, et al. Among authors: brais b. J Neurol. 2023 Dec;270(12):5784-5792. doi: 10.1007/s00415-023-11918-5. Epub 2023 Aug 14. J Neurol. 2023. PMID: 37578488

2

The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q.

Kibar Z, Der Kaloustian VM, Brais B, Hani V, Fraser FC, Rouleau GA. Kibar Z, et al. Among authors: brais b. Hum Mol Genet. 1996 Apr;5(4):543-7. doi: 10.1093/hmg/5.4.543. Hum Mol Genet. 1996. PMID: 8845850

3

Minimal expansion of the GCG repeat in the PABP2 gene does not predispose to sporadic inclusion body myositis.

Mezei MM, Mankodi A, Brais B, Marineau C, Thornton CA, Rouleau GA, Karpati G. Mezei MM, et al. Among authors: brais b. Neurology. 1999 Feb;52(3):669-70. doi: 10.1212/wnl.52.3.669. Neurology. 1999. PMID: 10025815 No abstract available.

4

Oculopharyngeal muscular dystrophy.

Brais B, Rouleau GA, Bouchard JP, Fardeau M, Tomé FM. Brais B, et al. Semin Neurol. 1999;19(1):59-66. doi: 10.1055/s-2008-1040826. Semin Neurol. 1999. PMID: 10711989 Review.

5

PABP2 polyalanine tract expansion causes intranuclear inclusions in oculopharyngeal muscular dystrophy.

Shanmugam V, Dion P, Rochefort D, Laganière J, Brais B, Rouleau GA. Shanmugam V, et al. Among authors: brais b. Ann Neurol. 2000 Nov;48(5):798-802. Ann Neurol. 2000. PMID: 11079546

6

Oculopharyngeal muscular dystrophy: What's new?

Codère F, Brais B, Rouleau G, Lafontaine E. Codère F, et al. Among authors: brais b. Orbit. 2001 Dec;20(4):259-266. doi: 10.1076/orbi.20.4.259.2617. Orbit. 2001. PMID: 12045902

7

HnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophy.

Fan X, Messaed C, Dion P, Laganiere J, Brais B, Karpati G, Rouleau GA. Fan X, et al. Among authors: brais b. Can J Neurol Sci. 2003 Aug;30(3):244-51. doi: 10.1017/s0317167100002675. Can J Neurol Sci. 2003. PMID: 12945950

8

Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein gene.

Stumpf E, Masson H, Duquette A, Berthelet F, McNabb J, Lortie A, Lesage J, Montplaisir J, Brais B, Cossette P. Stumpf E, et al. Among authors: brais b. Arch Neurol. 2003 Sep;60(9):1307-12. doi: 10.1001/archneur.60.9.1307. Arch Neurol. 2003. PMID: 12975300

9

Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians.

Roddier K, Thomas T, Marleau G, Gagnon AM, Dicaire MJ, St-Denis A, Gosselin I, Sarrazin AM, Larbrisseau A, Lambert M, Vanasse M, Gaudet D, Rouleau GA, Brais B. Roddier K, et al. Among authors: brais b. Neurology. 2005 May 24;64(10):1762-7. doi: 10.1212/01.WNL.0000161849.29944.43. Neurology. 2005. PMID: 15911806

10

A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34.

Thiffault I, Rioux MF, Tetreault M, Jarry J, Loiselle L, Poirier J, Gros-Louis F, Mathieu J, Vanasse M, Rouleau GA, Bouchard JP, Lesage J, Brais B. Thiffault I, et al. Among authors: brais b. Brain. 2006 Sep;129(Pt 9):2332-40. doi: 10.1093/brain/awl110. Epub 2006 May 3. Brain. 2006. PMID: 16672289

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

209 results

Search Page